8-Quinolinamine, 5-methoxy-


Chemical Name: 8-Quinolinamine, 5-methoxy-
CAS Number: 30465-68-0
Product Number: AG00306I(AGN-PC-0O8QZZ)
Synonyms:
MDL No:
Molecular Formula: C10H10N2O
Molecular Weight: 174.1992

Identification/Properties


Computed Properties
Molecular Weight:
174.203g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
174.079g/mol
Monoisotopic Mass:
174.079g/mol
Topological Polar Surface Area:
48.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
174
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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NMR Spectrum


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Chemical Structure



5-Methoxyquinolin-8-amine, also known as $name$, holds a crucial role in chemical synthesis as a versatile building block in organic chemistry. Its unique molecular structure and reactivity make it a valuable tool for creating various compounds and materials with diverse applications. $name$ is commonly used as a starting material in the synthesis of complex organic molecules, such as pharmaceuticals, agrochemicals, and functional materials. Its presence in the chemical synthesis process enables the introduction of specific functional groups or molecular scaffolds, allowing chemists to tailor the properties of the final product to meet desired specifications.One of the key applications of 5-Methoxyquinolin-8-amine is in the construction of heterocyclic compounds, which are essential components in many biologically active molecules. By incorporating $name$ into a synthetic pathway, chemists can access a wide range of heterocyclic structures that exhibit diverse pharmacological activities or serve as key intermediates for further functionalization.Additionally, 5-Methoxyquinolin-8-amine can be utilized for the preparation of fluorescent dyes, ligands for transition metal catalysts, and other specialized materials with specific properties. Its ability to participate in various chemical reactions, such as nucleophilic substitution, aromatic substitution, and metal-catalyzed coupling reactions, makes it a valuable asset in the toolbox of synthetic chemists.Overall, the use of 5-Methoxyquinolin-8-amine in chemical synthesis offers researchers a powerful platform to access structurally diverse compounds and functional materials, advancing the field of organic chemistry and enabling the creation of innovative products across industries.